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19

Clinical Protocol Writer Jobs






Job info
 
Company
Bristol-Myers Squibb Company
Location
Princeton, NJ
Posted Date
May 22, 2020
Info Source
Employer  - Full-Time  90  

... Bristol Myers Squibb Senior Scientific Writer in Princeton New Jersey Bristol-Myers ... transformative business results. Senior Scientific Writer - Clinical Study Protocols, Immuno‑Oncology and/or Specialty ... Specialty Position Objective:..

 
Company
**********
Location
, ,
Posted Date
Jun 10, 2020
Info Source
Recruiter  - Full-Time  90  

... two Healthcare Roles: 1) Medical/Regulatory Writer 2) Healthcare Managers Hello - ... candidates in each role: MEDICAL/REGULATORY WRITER 1) Senior-level Medical/Regulatory Writer: Candidates will need this background ... of..

 
Company
**********
Location
Hopewell, NJ
Posted Date
Jun 13, 2020
Info Source
Employer  - Full-Time  90  

... and key findings/messages. Authors complex clinical documents (e.g. protocols, phase II/III ... documents (e.g. protocols, phase II/III clinical study reports, high level summary ... level summary documents), and certain..

 
Company
**********
Location
Cambridge, MA
Posted Date
Feb 27, 2022
Info Source
Employer  - Full-Time  90  

... serve as an Associate Medical Writer to support clinical project teams to meet their ... project teams to meet their clinical document deliverables. The successful candidate ... Do: Serve..

 
Company
**********
Location
Mounds View, MN
Posted Date
Mar 01, 2022
Info Source
Employer  - Full-Time  90  

... portfolio at Medtronic. The **Senior Clinical Evidence Specialist** oversees the clinical evaluation process for cardiac medical ... devices in compliance with applicable clinical and regulatory standards and in .....

 
Company
Astellas Us, LLC
Location
Seattle, WA
Posted Date
Sep 03, 2022
Info Source
Employer  - Full-Time  90 

... regenerative medicine therapies. We conduct clinical-grade gene editing of stem cells ... announcing a RA II -- Clinical Gene Editing opportunity at their ... the Research Associate II for..

 
Company
**********
Location
Minneapolis, MN
Posted Date
Mar 01, 2022
Info Source
Employer  - Full-Time  90  

... portfolio at Medtronic. The **Principal Clinical Evidence Specialist** oversees the clinical evaluation process for cardiac medical ... devices in compliance with applicable clinical and regulatory standards and in .....

 
Company
**********
Location
Boston, MA
Posted Date
Feb 25, 2022
Info Source
Employer  - Full-Time  90 

... quality standards. The Senior Medical Writer is responsible for performing, preparing, ... for performing, preparing, and maintaining Clinical Evaluation Reports and PMCF documentation ... for medical devices and preparing..

 
Company
**********
Location
, ,
Posted Date
Mar 02, 2022
Info Source
Employer  - Full-Time  90  

... Park location. RESPONSIBILITIESThe Scientific Technical Writer/Editor’s primary responsibility will be to ... study reports, the Scientific Technical Writer/Editor will contribute to developing Technical ... to life sciences research (pharma,..

 
Company
**********
Location
Seattle, WA
Posted Date
Jun 13, 2020
Info Source
Employer  - Full-Time  90  

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..

 
Company
**********
Location
Shawnee, KS
Posted Date
Mar 01, 2022
Info Source
Employer  - Full-Time  90  

... is seeking a Sr Technical Writer to assist in writing scientific ... of drug development, preclinical and clinical studies.nIn this role, we will ... of drug developments, preclinical and..

 
Company
**********
Location
South San Francisco, CA
Posted Date
Feb 25, 2022
Info Source
Employer  - Full-Time  90  

... (NASDAQ: IDYA) is a public, clinical-stage synthetic lethality-focused precision medicine oncology ... to drive a more robust clinical response.IDEAYA recently announced a landmark ... well-organized, and skilled Senior Medical..

 
Company
**********
Location
, ,
Posted Date
Feb 22, 2022
Info Source
Employer  - Full-Time  90  

... while driving improved operational performance.The Clinical Data Analyst is responsible for ... activities in support of assigned clinical studies. Ensures that quality of ... responsible for writing and editing..

 
Company
**********
Location
, ,
Posted Date
Oct 25, 2022
Info Source
Recruiter  - Full-Time  90  

Recruiter for Medical Writer Hello - Im looking for a skilled recruiter to find Medical/Regulatory writers with a PhD. They must have the following skills: Candidates will need this background to ..

 
Company
BioMarin Pharmaceutical Inc.
Location
San Rafael, CA
Posted Date
Jun 18, 2023
Info Source
Employer  - Full-Time  90  

Who We Are From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work ..

 
Company
**********
Location
Berkeley Heights, NJ
Posted Date
Jul 09, 2020
Info Source
Employer  - Full-Time  90  

... and key findings/messages. Authors complex clinical documents (e.g. protocols, phase II/III ... documents (e.g. protocols, phase II/III clinical study reports, high level summary ... level summary documents), and certain..

 
Company
**********
Location
, ,
Posted Date
Feb 27, 2022
Info Source
Employer  - Full-Time  90  

... an Imaging Research and Imaging Clinical Research Organization (iCRO) that also ... trials, particularly within oncology.The Principal Writer, Medical and Scientific Affairs is ... medical writing services at a..

 
Company
Astellas Us, LLC
Location
Seattle, WA
Posted Date
Sep 23, 2022
Info Source
Employer  - Full-Time  90 

22-POS00030628 - Technical Lead or Group Lead Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to ..

 
Company
**********
Location
, ,
Posted Date
Oct 25, 2022
Info Source
Recruiter  - Full-Time  90  

Regulatory/Medical Writers Looking for senior-level (5 years medical/regulatory writing experience) for Medical Writer positions. You MUST be a PhD in Medical and have pharma experience -Must have regulatory experience and writing ..

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